Immunocytochemical localization of the cystic fibrosis gene product CFTR. - Wikidata - awgldk - TriplyDB

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

http://www.wikidata.org/entity/Q37609030

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Distribution of aquaporin water channels AQP1 and AQP5 in the ductal system of the human pancreas Two highly homologous members of the ClC chloride channel family in both rat and human kidney The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70 Binding of serum response factor to cystic fibrosis transmembrane conductance regulator CArG-like elements, as a new potential CFTR transcriptional regulation pathway.Chromatin Dynamics in the Regulation of CFTR Expression Molecular mechanism of pancreatic and salivary gland fluid and HCO3 secretion Assembly and trafficking of a multiprotein ROMK (Kir 1.1) channel complex by PDZ interactions Endoplasmic reticulum membrane-sorting protein of lymphocytes (BAP31) is highly expressed in neurons and discrete endocrine cells The stoichiometry of the electrogenic sodium bicarbonate cotransporter pNBC1 in mouse pancreatic duct cells is 2 HCO(3)(-):1 Na(+)Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct Interaction between CFTR and prestin (SLC26A5)Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte.Immunolocalization and regulation of cystic fibrosis transmembrane conductance regulator in the adult rat epididymis.Tissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTR CFTR and TNR-CFTR expression and function in the kidney.Structure and function of the cystic fibrosis transmembrane conductance regulator.Molecular diversity and regulation of renal potassium channels.A mild variant of cystic fibrosis.A PDZ-interacting domain in CFTR is an apical membrane polarization signal.The multidrug resistance and cystic fibrosis genes have complementary patterns of epithelial expression.Respiratory syncytial virus engineered to express the cystic fibrosis transmembrane conductance regulator corrects the bioelectric phenotype of human cystic fibrosis airway epithelium in vitro.The cystic fibrosis transmembrane regulator (CFTR) in the kidney.Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells.Renal tubule potassium channels: function, regulation and structure.Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.Cystic fibrosis in adults. From researcher to practitioner.Uroguanylin: structure and activity of a second endogenous peptide that stimulates intestinal guanylate cyclase.Reversal of cystic fibrosis phenotype in a cultured Delta508 cystic fibrosis transmembrane conductance regulator cell line by oligonucleotide insertion.Renal vacuolar H+-ATPase.Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.Molecular analysis of the ovine cystic fibrosis transmembrane conductance regulator gene.WNK4-mediated regulation of renal ion transport proteins.Low abundance of sweat duct Cl- channel CFTR in both healthy and cystic fibrosis athletes with exceptionally salty sweat during exercise.Chloride channels in the kidney: lessons learned from knockout animals.Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes.Intestinal ion transport and the pathophysiology of diarrhea CFTR!F508del-cystic fibrosis transmembrane regulator correctors for treatment of cystic fibrosis: a patent review.Nucleosome occupancy reveals regulatory elements of the CFTR promoter.Differential cellular expression of cystic fibrosis transmembrane regulator in human reproductive tissues. Clues for the infertility in patients with cystic fibrosis.

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P2860

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

http://www.wikidata.org/entity/Q37609030

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on October 1991

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@en

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@nl

type

label

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@en

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@nl

prefLabel

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@en

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

@nl

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PNAS.88.20.9262

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Immunocytochemical localization of the cystic fibrosis gene product CFTR.

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P2093

Crawford I

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Gatter KC

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Guggino WB

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Harris A

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Higgins CF

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Hyde SC

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Maloney PC

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Turley H

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Zeitlin PL

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P2860

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

Molecular cloning of the CD2 antigen, the T-cell erythrocyte receptor, by a rapid immunoselection procedure

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

Chloride impermeability in cystic fibrosis.

Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator.

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.

P304

9262-9266

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scholarly article

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10.1073/PNAS.88.20.9262

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20

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88

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1991-10-01T00:00:00Z

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21437785

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1718002

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P921

cystic fibrosis

P932

52694

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